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SARS-CoV-2 reinfection prevents acute respiratory disease in Syrian hamsters but not replication in the upper respiratory tract
Human cases of SARS-CoV-2 reinfection have been documented throughout the pandemic, but are likely under-reported. In the current study, we use the Syrian hamster SARS-CoV-2 model to assess reinfection with homologous WA1 and heterologous B.1.1.7 (Alpha) and B.1.351 (Beta) SARS-CoV-2 variants over t...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8860630/ https://www.ncbi.nlm.nih.gov/pubmed/35263638 http://dx.doi.org/10.1016/j.celrep.2022.110515 |
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author | Hansen, Frederick Meade-White, Kimberly Clancy, Chad Rosenke, Rebecca Okumura, Atsushi Hawman, David W. Feldmann, Friederike Kaza, Benjamin Jarvis, Michael A. Rosenke, Kyle Feldmann, Heinz |
author_facet | Hansen, Frederick Meade-White, Kimberly Clancy, Chad Rosenke, Rebecca Okumura, Atsushi Hawman, David W. Feldmann, Friederike Kaza, Benjamin Jarvis, Michael A. Rosenke, Kyle Feldmann, Heinz |
author_sort | Hansen, Frederick |
collection | PubMed |
description | Human cases of SARS-CoV-2 reinfection have been documented throughout the pandemic, but are likely under-reported. In the current study, we use the Syrian hamster SARS-CoV-2 model to assess reinfection with homologous WA1 and heterologous B.1.1.7 (Alpha) and B.1.351 (Beta) SARS-CoV-2 variants over time. Upon primary infection with SARS-CoV-2 WA1, hamsters rapidly develop a strong and long-lasting humoral immune response. After reinfection with homologous and heterologous SARS-CoV-2 variants, this immune response protects hamsters from clinical disease, virus replication in the lower respiratory tract, and acute lung pathology. However, reinfection leads to SARS-CoV-2 replication in the upper respiratory tract with the potential for virus shedding. Our findings indicate that reinfection results in restricted SARS-CoV-2 replication despite substantial levels of humoral immunity, denoting the potential for transmission through reinfected asymptomatic individuals. |
format | Online Article Text |
id | pubmed-8860630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-88606302022-02-22 SARS-CoV-2 reinfection prevents acute respiratory disease in Syrian hamsters but not replication in the upper respiratory tract Hansen, Frederick Meade-White, Kimberly Clancy, Chad Rosenke, Rebecca Okumura, Atsushi Hawman, David W. Feldmann, Friederike Kaza, Benjamin Jarvis, Michael A. Rosenke, Kyle Feldmann, Heinz Cell Rep Article Human cases of SARS-CoV-2 reinfection have been documented throughout the pandemic, but are likely under-reported. In the current study, we use the Syrian hamster SARS-CoV-2 model to assess reinfection with homologous WA1 and heterologous B.1.1.7 (Alpha) and B.1.351 (Beta) SARS-CoV-2 variants over time. Upon primary infection with SARS-CoV-2 WA1, hamsters rapidly develop a strong and long-lasting humoral immune response. After reinfection with homologous and heterologous SARS-CoV-2 variants, this immune response protects hamsters from clinical disease, virus replication in the lower respiratory tract, and acute lung pathology. However, reinfection leads to SARS-CoV-2 replication in the upper respiratory tract with the potential for virus shedding. Our findings indicate that reinfection results in restricted SARS-CoV-2 replication despite substantial levels of humoral immunity, denoting the potential for transmission through reinfected asymptomatic individuals. Cell Press 2022-03-15 2022-02-22 /pmc/articles/PMC8860630/ /pubmed/35263638 http://dx.doi.org/10.1016/j.celrep.2022.110515 Text en Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Hansen, Frederick Meade-White, Kimberly Clancy, Chad Rosenke, Rebecca Okumura, Atsushi Hawman, David W. Feldmann, Friederike Kaza, Benjamin Jarvis, Michael A. Rosenke, Kyle Feldmann, Heinz SARS-CoV-2 reinfection prevents acute respiratory disease in Syrian hamsters but not replication in the upper respiratory tract |
title | SARS-CoV-2 reinfection prevents acute respiratory disease in Syrian hamsters but not replication in the upper respiratory tract |
title_full | SARS-CoV-2 reinfection prevents acute respiratory disease in Syrian hamsters but not replication in the upper respiratory tract |
title_fullStr | SARS-CoV-2 reinfection prevents acute respiratory disease in Syrian hamsters but not replication in the upper respiratory tract |
title_full_unstemmed | SARS-CoV-2 reinfection prevents acute respiratory disease in Syrian hamsters but not replication in the upper respiratory tract |
title_short | SARS-CoV-2 reinfection prevents acute respiratory disease in Syrian hamsters but not replication in the upper respiratory tract |
title_sort | sars-cov-2 reinfection prevents acute respiratory disease in syrian hamsters but not replication in the upper respiratory tract |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8860630/ https://www.ncbi.nlm.nih.gov/pubmed/35263638 http://dx.doi.org/10.1016/j.celrep.2022.110515 |
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